Harding AE - Search Results

1

Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A-->G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA.

Hanna MG, Nelson IP, Morgan-Hughes JA, Harding AE. Hanna MG, et al. Among authors: harding ae. J Neurol Sci. 1995 Jun;130(2):154-60. doi: 10.1016/0022-510x(95)00022-t. J Neurol Sci. 1995. PMID: 8586979

2

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

Holt IJ, Harding AE, Morgan-Hughes JA. Holt IJ, et al. Among authors: harding ae. Nature. 1988 Feb 25;331(6158):717-9. doi: 10.1038/331717a0. Nature. 1988. PMID: 2830540

3

Mitochondrial DNA polymorphism in mitochondrial myopathy.

Holt IJ, Harding AE, Morgan-Hughes JA. Holt IJ, et al. Among authors: harding ae. Hum Genet. 1988 May;79(1):53-7. doi: 10.1007/BF00291710. Hum Genet. 1988. PMID: 2896621

4

Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study.

Brockington M, Alsanjari N, Sweeney MG, Morgan-Hughes JA, Scaravilli F, Harding AE. Brockington M, et al. Among authors: harding ae. J Neurol Sci. 1995 Jul;131(1):78-87. doi: 10.1016/0022-510x(95)00091-f. J Neurol Sci. 1995. PMID: 7561952

5

Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.

Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: harding ae. Biochim Biophys Acta. 1995 May 24;1271(1):135-40. doi: 10.1016/0925-4439(95)00020-5. Biochim Biophys Acta. 1995. PMID: 7599199 Free article.

6

The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.

Hammans SR, Sweeney MG, Hanna MG, Brockington M, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Among authors: harding ae. Brain. 1995 Jun;118 ( Pt 3):721-34. doi: 10.1093/brain/118.3.721. Brain. 1995. PMID: 7600089

7

A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study.

Nelson I, Hanna MG, Alsanjari N, Scaravilli F, Morgan-Hughes JA, Harding AE. Nelson I, et al. Among authors: harding ae. Ann Neurol. 1995 Mar;37(3):400-3. doi: 10.1002/ana.410370317. Ann Neurol. 1995. PMID: 7695240

8

Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.

Hanna MG, Nelson I, Sweeney MG, Cooper JM, Watkins PJ, Morgan-Hughes JA, Harding AE. Hanna MG, et al. Among authors: harding ae. Am J Hum Genet. 1995 May;56(5):1026-33. Am J Hum Genet. 1995. PMID: 7726155 Free PMC article.

9

Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy.

Sweeney MG, Hammans SR, Duchen LW, Cooper JM, Schapira AH, Kennedy CR, Jacobs JM, Youl BD, Morgan-Hughes JA, Harding AE. Sweeney MG, et al. Among authors: harding ae. J Neurol Sci. 1994 Jan;121(1):57-65. doi: 10.1016/0022-510x(94)90157-0. J Neurol Sci. 1994. PMID: 8133313

10

Mitochondrial DNA transfer RNA mutation Leu(UUR)A-->G 3260: a second family with myopathy and cardiomyopathy.

Sweeney MG, Brockington M, Weston MJ, Morgan-Hughes JA, Harding AE. Sweeney MG, et al. Among authors: harding ae. Q J Med. 1993 Jul;86(7):435-8. Q J Med. 1993. PMID: 8210299

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

251 results

Search Page

Filters